Zobrazeno 1 - 10
of 31
pro vyhledávání: '"José Ramón Vizcaíno"'
Autor:
Margarida Gonçalves, Helena Pessegueiro, Judit Gandara, José Ramón Vizcaíno, Vitor Lopes, Sofia Ferreira
Publikováno v:
GE: Portuguese Journal of Gastroenterology, Pp 1-5 (2023)
Epithelioid hemangioendothelioma is a very rare vascular neoplasm, which is often multifocal or metastatic at diagnosis. Most frequently arises in the liver, followed by the lung and bones. The authors present a case of a liver transplant recipient w
Externí odkaz:
https://doaj.org/article/7c39420e70964ee49751474ea2b7b7e4
Publikováno v:
Diagnostics, Vol 12, Iss 1, p 140 (2022)
Basaloid follicular hamartoma (BFH) is a normally benign, uncommon, malformative lesion involving the hair follicles, which usually poses challenges in the differential diagnosis with other benign and malignant tumours, especially basal cell carcinom
Externí odkaz:
https://doaj.org/article/3e8a768b4a6646edb02c424cf0e788db
Autor:
Pedro Azevedo, Cristina Freitas, Hugo Silva, Pedro Aguiar, Pedro Farrajota, Manuela Almeida, Sofia Pedroso, La Salete Martins, Leonídio Dias, José Ramón Vizcaíno, António Castro Henriques, António Cabrita
Publikováno v:
Case Reports in Nephrology, Vol 2013 (2013)
Tuberculosis is a disease relatively frequent in renal transplant patients, presenting a wide variety of clinical manifestations, often involving various organs and potentially fatal. Gastrointestinal tuberculosis, although rare in the general popula
Externí odkaz:
https://doaj.org/article/daa56f02c3f94a49ac8283d128e6971c
Autor:
David Tente, Joana Raposo Alves, José Ramón Vizcaíno, Francisca Emanuel Costa, Nuno Jorge Lamas, Sara Esteves, Paula Fonseca
Publikováno v:
Annals of Diagnostic Pathology
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
The coronavirus disease 2019 (COVID-19) pandemic has dramatically changed the world over the past weeks, with already 8,25 million infections and 445,000 deaths worldwide, leading to an unprecedented international global effort to contain the virus a
Publikováno v:
Cancer Cytopathology
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Submitted by José Pereira (jro.pereira@gmail.com) on 2021-11-12T12:05:56Z No. of bitstreams: 1 Lamas-2020-Liquidbased-cytology-specimen-prepa.pdf: 71450 bytes, checksum: 6fa54b20d9d484472b1f9cbbea9963bc (MD5) Made available in DSpace on 2021-11-12T1
Publikováno v:
Open Journal of Pathology. :13-19
Background: Porto’s Hospital Centre is one of the most active Portuguese hospitals in renal transplantation (performed since 1983). Although increasingly rare, opportunistic infections in transplanted patients are associated with high mortality rat
Autor:
Rui Henrique, Justin A. Bishop, Alfio Ferlito, Fernando Pardal, Nicole A. Cipriani, Henrik Hellquist, Andrés Coca-Pelaz, Evan J. Propst, Christopher A. French, Ronald Grant, Bo-Yee Ngan, David Vokes, José Ramón Vizcaíno, Alessandra Rinaldo, António Paiva Correia
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
AIMS: NUT midline carcinoma (NMC) is a rare undifferentiated and aggressive carcinoma that locates characteristically to the midline of the head and neck, and mediastinum. NMC is characterized by chromosomal rearrangements of the gene NUT, at 15q14.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80f9adad2e6f1cd0a05d522b8d591d7f
Autor:
Luis Martí-Bonmatí, Angel Alberich-Bayarri, M. França, Sara Vieira Silva, H. Pessegueiro Miranda, Graça Porto, José Ramón Vizcaíno, S. Guimarães
Publikováno v:
CLINICAL RADIOLOGY
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Aim: To investigate iron loading within the liver, pancreas, spleen, and bone marrow using magnetic resonance imaging (MRI) transverse relaxation rate (R2*), in patients with diffuse liver diseases; to evaluate the relationships between iron accumula
Autor:
Ricardo Ribeiro, Carlos Lobato, André Coelho, José Manuel Lopes, José Ramón Vizcaíno, Rui Medeiros, Paulo Príncipe, Helena Coutinho, Avelino Fraga, Carlos Lopes
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
BMC Urology
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
BMC Urology
Background In this study we sought if, in their quest to handle hypoxia, prostate tumors express target hypoxia-associated molecules and their correlation with putative functional genetic polymorphisms. Methods Representative areas of prostate carcin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0f961a336b87fae75a050076074f3a3
https://hdl.handle.net/10400.16/2170
https://hdl.handle.net/10400.16/2170
Autor:
Fernando Neves, Guy Froyen, S. Alves, Umbelina Ramos, Maria João Nabais Sá, Márcia Rodrigues, Fernando Teixeira e Costa, Nathalie Fieremans, Adelino Carvalho, Arjan P.M. de Brouwer, Maria José Brito, Joana Felgueiras, Fernanda Carvalho, Rita de Sousa, Francisco Sousa, José Ramón Vizcaíno, Filipa Carvalho, João Paulo Oliveira
Publikováno v:
Journal of Medical Genetics, 50, 11, pp. 745-53
Journal of Medical Genetics, 50, 745-53
Journal of Medical Genetics, 50, 745-53
Background Alport syndrome (AS), a hereditary type IV collagen nephropathy, is a major cause of end-stage renal disease in young people. About 85% of the cases are X-linked (ATS), due to mutations in the COL4A5 gene. Rarely, families have a contiguou